US9908642B1 - Biologically inspired radiation reflector - Google Patents
Biologically inspired radiation reflector Download PDFInfo
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- US9908642B1 US9908642B1 US14/604,553 US201514604553A US9908642B1 US 9908642 B1 US9908642 B1 US 9908642B1 US 201514604553 A US201514604553 A US 201514604553A US 9908642 B1 US9908642 B1 US 9908642B1
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B64—AIRCRAFT; AVIATION; COSMONAUTICS
- B64G—COSMONAUTICS; VEHICLES OR EQUIPMENT THEREFOR
- B64G1/00—Cosmonautic vehicles
- B64G1/22—Parts of, or equipment specially adapted for fitting in or to, cosmonautic vehicles
- B64G1/52—Protection, safety or emergency devices; Survival aids
- B64G1/54—Protection against radiation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B64—AIRCRAFT; AVIATION; COSMONAUTICS
- B64G—COSMONAUTICS; VEHICLES OR EQUIPMENT THEREFOR
- B64G1/00—Cosmonautic vehicles
- B64G1/22—Parts of, or equipment specially adapted for fitting in or to, cosmonautic vehicles
- B64G1/52—Protection, safety or emergency devices; Survival aids
- B64G1/58—Thermal protection, e.g. heat shields
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/90—Carbides
- C01B32/914—Carbides of single elements
- C01B32/956—Silicon carbide
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/62605—Treating the starting powders individually or as mixtures
- C04B35/62685—Treating the starting powders individually or as mixtures characterised by the order of addition of constituents or additives
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B64—AIRCRAFT; AVIATION; COSMONAUTICS
- B64G—COSMONAUTICS; VEHICLES OR EQUIPMENT THEREFOR
- B64G1/00—Cosmonautic vehicles
- B64G1/22—Parts of, or equipment specially adapted for fitting in or to, cosmonautic vehicles
- B64G1/62—Systems for re-entry into the earth's atmosphere; Retarding or landing devices
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3418—Silicon oxide, silicic acids or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/40—Metallic constituents or additives not added as binding phase
- C04B2235/401—Alkaline earth metals
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/46—Gases other than oxygen used as reactant, e.g. nitrogen used to make a nitride phase
Definitions
- This invention relates to use of innovative materials in a thermal protection system (TPS) for a re-entry vehicle.
- TPS thermal protection system
- RV surface heating has two primary sources (1) convective heating (proportional to (velocity) 3 )from flow of hot gases past the surface and from chemical combination reactions in the gases; and (2) radiation heating (approximately proportional to (velocity) 8 ) from a shock wave that forms preceding the RV).
- Radiative heating of an RV and its heat shield peaks early in a re-entry interval into an atmosphere, and this heating often arises from specific, limited ranges of wavelengths of concern, ⁇ rad ⁇ , dependent upon atmospheric composition, as indicated in FIG. 1 .
- Provision of a heat shield that has an approximately periodic structure that is preferentially reflective for wavelengths in the range ⁇ rad ⁇ would reduce the fraction of radiation that contacts the RV surface.
- construction of such a heat shield is likely to be expensive and technically demanding.
- the primary heat shield material is refractory and has a high phase change temperature for ablating.
- the invention provides a new heat shield material that: (1) is initially a natural material with a quasi-periodic pore sub-structure; and (2) is processed to form a refractory mixture (e.g., SiC and SiO x ) with superior radiation reflection, phase change and thermal characteristics over the wavelength range ⁇ rad ⁇ .
- MgO is leached from the diatom structure with an acid to form a pure Si frustule.
- the frustule is then reacted with H 2 and a hydrocarbon gas, such as CH 4 or C 2 H 4 or C 2 H 6 , to form a mixture of SiO x and SiC (crystalline and/or amorphous), with the degree of crystallinity being estimatable by X-ray diffraction.
- MgO is formed in preference to formation of either of the compounds, MgSi and/or MgSiO 4 , which would resist removal of the Mg.
- a heat shield material additive comprising a mixture of SiC and SiO x with a quasi-periodic diatom pore structure and prepared in this manner, may have a high phase change temperature (melting, ablation, evaporation, sublimation, etc.), and has a bulk optical reflectivity OR of at least about 0.19 or 0.033 for normal incidence. Incident radiation may also be photonically reflected at much higher values of OR. Other processing details are discussed in a Description of the Invention.
- the optical reflectivity value OR tends to increase with increasing incidence angle of radiation received at the heat shield component.
- the additive may be a continuous layer.
- the additive is incorporated onto an exposed surface of the substrate heat shield material by impregnation, coating or similar techniques that may produce non-continuous or isolated deposits the additive.
- This reflecting additive layer would be operate primarily during an initial time interval (e.g., the first 30-60 sec of re-entry).
- FIG. 1 graphically presents an estimate of a radiation spectrum provided by shock layer atomic line radiance (ALR), as a function of wavelength ⁇ for an assumed shock layer temperature T(rad;SL)) ⁇ 10,000° C. and a corresponding estimated heat shield temperature T(rad;HS) ⁇ 4,000° C., in an environment that is initially substantially free of atomic oxygen;
- ALR shock layer atomic line radiance
- FIG. 2 schematically illustrates an FBR conversion method used here.
- FIGS. 3A and 3B graphically present refractive indices n( ⁇ ;T) for SiC and for SiO x for visible and mid-infrared wavelengths ⁇ .
- FIG. 4 indicates graphically a development of temperature adjacent to a temperature at which phase change occurs (melting, ablation, evaporation, sublimation, etc.), according to a conventional view.
- FIG. 5 graphically presents an estimation of solution of heat equation for a semi-infinite, one dimensional solid with radiation input at a boundary.
- FIG. 6 illustrates reflection/re-radiation that is examined here.
- the invention relies for the initial (natural) material upon diatoms containing diatomite (diatomaceous earth), a sedimentary rock composed of fossilized skeletons of diatoms, which are one-celled, algae-like, micron-sized, mostly photosynthetic phytoplankton.
- Diatomite composition is mainly amorphous SiO x , with a quasi-periodic arrangement of inter-connected pores of nanometer size. These quasi-periodic structures give diatomite some useful photon interaction characteristics.
- Each diatom is bounded by a silica frustule or cell wall, including two valves of slightly different size that fit together in a connective zone, known as a girdle, and enclose the remainder of a diatom.
- An estimated 100,000 species of diatoms are extant in the oceans, usually restricted to the photic zone.
- Diatom diameters normally range from 40 nm to 200 ⁇ m, with pore-to-pore separations that are consistent with a preferred wavelength range ⁇ rad ⁇ .
- the diatoms initially comprise SiO x .
- a goal here is to transform the diatoms into a material with higher phase change temperature, while retaining a quasi-periodic pore structure within a diatom that provides an enhanced photon-reflecting structure.
- the transformation or conversion process begins with addition of Mg(gas) to a powder bed of diatom frustules, which comprise SiO x , (x ⁇ 1) in a heated Fluid Bed Reactor (FBR) at a temperature T(FBR) ⁇ 600° C.
- FBR Fluid Bed Reactor
- Mg(solid) is heated and Mg(gas) particles react with SiO 2 to form MgO in a first reaction, 2Mg(gas)+SiO 2 +Ar ⁇ Si(solid)+2MgO(solid)+Ar.
- MgO is leached from the diatom structure with HCl or another modest strength acid to provide frustule structures containing primarily Si, Si+MgO+2HCl+Ar ⁇ Si+MgCl 2 +H 2 O+Ar, (2)
- the Si frustule is reacted with a hydrocarbon gas (CH 4 , C 2 H 4 , C 2 H 6 , etc,) and with H 2 gas in the FBR to form an SiC frustule, Si+CH 4 +H 2 Ar ⁇ SiC+3H 2 +Ar. (3-1) 2Si+C 2 H 4 +H 2 +Ar ⁇ 2SiC+3H 2 +Ar. (3-2) 2Si+C 2 H 6 +H 2 +Ar ⁇ 2SiC+4H 2 +Ar. (3-3) An assembly of SiC frustules, formed at temperatures (T ⁇ 800° C., preferably T ⁇ 650° C.), will likely be amorphous.
- a hydrocarbon gas CH 4 , C 2 H 4 , C 2 H 6 , etc,
- SiC frustules formed in the third reaction (3-1,2,3) will require higher temperatures to increase crystallinity fraction. Conversion to SiC frustules may be faster and use lower temperatures than normal. Conversion of the SiO x to SiC by this process may not be complete so that the substances produced by this process may be a mixture comprising SiC and SiO x .
- FIG. 2 schematically represents a Fluidized Bed Reactor (FBR) 21 that can be used for the transformation of the diatom powder to SiC and SiO x .
- the FBR includes a quartz reactor vessel 22 that facilitates the three reactions set forth in Eqs. (1), (2) and (3-1) or (3-2) Or (3-3).
- a fluidized powder bed 23 provides an initial reaction site. Reactant gases are received by the bed from a reactant source 24 and passed through the bed, together with a fluidizing gas from a fluidizing source 25 . Heat is provided by a high temperature source 26 . The resulting gases are drawn off through a vent 27 .
- Processing parameters are continually adjusted in attempting to optimize the partial or total conversion of amorphous SiO x frustules to SiC. Pore structure and almost-periodic atomic structure are maintained, but further improvements are needed to achieve full conversion to SiC; some SiO x may remain in the mix.
- SiC polytype(s) will be produced by the frustule reactions set forth in the preceding first, second and third reactions.
- the Si that may result from the process set forth in Eqs. (1), (2) and (3) has a melt temperature range T(melt) ⁇ 1414° C. and an evaporation temperature T(evap) ⁇ 3265° C.
- a first estimate of optical reflectivity OR( ⁇ ;T) associated with the first sublayer SubL assumes that all sublimated SiC material is promptly removed from a region adjacent to SubL and that the local environment comprises a heated first sublayer material with an associated refractive index n( ⁇ ;T) and a contiguous second layer that is substantially a vacuum, with associated refractive index n ⁇ 1, as illustrated in FIG. 3A .
- FIG. 3B graphically illustrates variation of refractive index n( ⁇ ;T;SiO x ) with wavelength for a wavelength range of interest here.
- SiO x is the bulk material
- the optical reflectivity OR( ⁇ ;T) of a block of material may be enhanced by choosing a diatom species with nearest neighbor pore separation distances d(p-p) (measured laterally) having selected values that are approximately equal to optimal values estimated in the technical literature.
- d(p-p) nearest neighbor pore separation distances
- an additive material is a mixture of SiC and SiO x , enhanced reflection of wavelengths in corresponding first and second wavelength ranges are likely, with possible further reflection enhancement relative to an additive that contains only SiC or only SiO x , because of broader coverage of the wavelength ranges affected.
- the pore-to-pore separation distances d(p-p) will not be precisely the same so that the arrangement of pores will be quasi-periodic rather than strictly periodic.
- the transformed diatom material (SiC or SiO x ) is provided as a coating or first sub-layer SubL, located at an exposed surface of the heat shield, and experiences an estimated maximum temperature, from shock layer radiation and convective heating, T(rad;max;1) ⁇ 4000° C. This maximum HS surface temperature subsequently decreases to lower temperatures over the next 30-60 sec. A first portion of the first sub-layer undergoes phase change in this environment and is treated here as providing no substantial contribution to reflection of radiation received from the shock layer SL.
- a second (remaining) portion of the first sub-layer is assumed to be intact and to have sufficient (remaining) longitudinal thickness ⁇ h to provide an associated optical reflectivity, OR( ⁇ ;T) ⁇ 0.19 or 0.033, for this second (remaining) portion of the first sub-layer SubL.
- Phase change of a volume ⁇ V of SiC or SiO x requires provision of at least the following radiant energy: (i) a first energy density component ⁇ E1 that is required to raise the volume ⁇ V from a reference temperature value T(ref) to a phase change initiation temperature T(phase), and (ii) a second measure of energy input ⁇ E 2 required to convert the volume ⁇ V of initially solid SiC or SiO x material at temperature T(phase) to material that has undergone a phase change.
- T(ref) a reference temperature value
- a second measure of energy input ⁇ E 2 required to convert the volume ⁇ V of initially solid SiC or SiO x material at temperature T(phase) to material that has undergone a phase change.
- FIG. 4 according to a conventional view. This perspective applies for phase change of a volume of SiC or of SiO x .
- the local heat energy ( ⁇ c)u(x,t) When the local heat energy ( ⁇ c)u(x,t) reaches a value ⁇ E1, the temperature in a local volume ⁇ V has reached a first value at which the phase change process begins. However, the local heat energy ( ⁇ c)u(x,t) must reach an energy value, ⁇ E1+ ⁇ E 2 , in order to complete the phase change process in the local volume ⁇ V. This analysis will focus primarily on the total energy, ⁇ E1+ ⁇ E2 required to complete the phase change process in the local volume ⁇ V.
- a volume ⁇ V located at a coordinate x corresponding to s>0.27, cannot (yet) complete the phase change.
- the numerical value of the fraction ⁇ of maximum heat energy actually chosen will depend upon the power density value provided by the shock layer radiation and upon the total energy, ⁇ E1+ ⁇ E2 , required for completion of phase change for the volume ⁇ V.
- the portion of the solid for which the phase change process is completed may pass away as a gas or vapor so that an initial thickness value ⁇ of the SiC or SiO x material will decrease as time increases.
- the portion of the thickness ⁇ that does not survive the phase change process serves as a sacrificial layer.
- the SiC and/or SiO x material is deposited in isolated clusters at an exposed surface of another heat shield component on an RV, through impregnation or other deposit process.
- An estimate of overall optical reflectivity for the exposed surface (area A) of the heat shield then becomes
- the invention disclosed here incorporates diatom material, transformed or converted into SiC and/or SiO x , as an additive in a heat shield component in order to enhance the thermal protection characteristics in at least one of two ways: (1) increasing temperatures or heat content required for phase change of the material and enhancing refractory behavior of the material; and (2) enhancing photonic behavior and reflection of radiation received by the shield from a shock layer that forms as the RV enters or re-enters the atmosphere of a planetary body.
- the pore structure within a diatom is quasi-periodic, and an average nearest neighbor pore-to-pore separation distance d(p-p) is preferably chosen to be approximately equal to one or more of the estimated optimal periodicity dimensions.
- the heat content received by the heat shield and its additive comprises radiation from a shock layer that forms upon RV entry or re-entry and convective heating produced by motion of the RV.
- the additive provides (i) enhanced reflection of the radiation of wavelengths in a range that corresponds to wavelengths of the incident radiation and (ii) re-radiation of the convective heating received, at wavelengths that are generally larger than the range of wavelengths that are associated with convective heating.
- a primary goal is to reduce substantially the convective and radiation heat content that is ultimately absorbed by the heat shield and additive.
- the diatom material that is processed to provide the additive is initially a naturally occurring material with a quasi-periodic pore structure within each diatom.
- the reflection of radiation in an associated wavelength range and re-radiation of wavelengths in another (convective heating) range are separately illustrated in FIG. 6 .
- Diatoms are unicellular, eukaryotic, mostly photosynthetic micro-organisms that possess exoskeletons (frustules) comprising amorphous silica (SiO x ). Each diatom is bounded by a frustule or cell wall of silica (hydrated SiO x ), including two valves of slightly different size that fit together in a connective zone, known as a girdle, and enclose the remainder of a diatom. Diameters of the diatoms lie in a range 2-2,000 ⁇ m; some species can be seen with an unaided eye. An estimated 100,000 species of diatoms are extant in the oceans, usually restricted to the photic zone (extending to a depth of about 200 feet).
- Diatom reproduction is primarily asexual, by binary fission.
- a typical diatom may have about 11,000 genes.
- diatoms represent as much as 70 percent of the phytoplankton community and produce about 25 percent of the oxygen on the Earth. A bloom cycle will often terminate because of depletion of available silicon.
- Diatoms are traditionally divided into two orders: Centrales or centric diatoms have pores or apertures that are distributed approximately radially symmetric; and Pennate diatoms have pores or apertures that are distributed approximately bilaterally symmetric. Diatoms of the same species consistently form shells or frustules with the same pattern, which may indicate that the designs are genetically programmed. Frustules of a diatom will usually have pores or apertures, often with pore diameter values d(pore) of about 40 nm, but with nearest neighbor pore separation distances d(p-p) that have a larger range. The limited range of pore diameters d(pore) allows diatom frustules to be used for particle sorting and separation.
- a hydrofluoric acid (HF) solution can be used to increase the pore diameters d(pore) for a given diatom. It is unclear what effect, if any, an HF treatment has on the pore-to-pore separation distance d(p-p).
- porous layers of silica are present, and the pore distribution is approximately linear (row upon row, referred to as “concentric”), rather than radially symmetric. Pore-to-pore separation distances within an individual diatom can be as large as about 2 ⁇ m.
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Abstract
Description
2Mg(gas)+SiO2+Ar →Si(solid)+2MgO(solid)+Ar. (1)
We have found that use of high heating rates in this reaction, together with extended temperature pauses at T≧850° C., produce competing magnesium silicides (MgSi) and magnesium silicates (MgSiO4), which are compounds that will not leach or surrender the Mg (undesirable). Use of moderate temperatures, preferably no higher than T=640-800° C. and for no longer than a selected time interval, Δt1=8 hours, in this reaction, are preferred. Particle size of the Mg reactant is important. Use of smaller diameter Mg particles (dia≦100 μm) allows use of lower temperature ramp rates and a longer low temperature pause, with T≦600° C., which avoids or minimizes damaging exothermic reactions.
Si+MgO+2HCl+Ar→Si+MgCl2+H2O+Ar, (2)
Si+CH4+H2Ar→SiC+3H2+Ar. (3-1)
2Si+C2H4+H2+Ar→2SiC+3H2+Ar. (3-2)
2Si+C2H6+H2+Ar→2SiC+4H2+Ar. (3-3)
An assembly of SiC frustules, formed at temperatures (T≦800° C., preferably T≦650° C.), will likely be amorphous. SiC frustules formed in the third reaction (3-1,2,3) will require higher temperatures to increase crystallinity fraction. Conversion to SiC frustules may be faster and use lower temperatures than normal. Conversion of the SiOx to SiC by this process may not be complete so that the substances produced by this process may be a mixture comprising SiC and SiOx.
OR(λ;T)={(n(λ;T)−1)/(n(λ;T)+1)}2, (4)
which has a value of about 0.204 for room temperature SiC and for a wavelength λ=589 nm. This ignores a small difference between ordinary and extraordinary refractive indices, no=2.648 and ne=2.691, of SiC at these conditions. Estimates of variation of refractive index n(λ;T) with wavelength λ for bulk SiC, illustrated in
λ(mm)T(°K)=0.00289, (5)
with an assumed temperature of T=4273° K. The wavelength range {λrad} of interest in this situation is approximately 190 nm (vacuum uv)≦λ≦3000 nm so that use of a refractive index, n(λ;T)≧2.55, with associated bulk SiC optical reflectivity, OR(λ;T;SiC)=0.19, appears to be reasonable for modest temperatures.
∂2 u/∂x 2−(1/κ)∂u/∂t=0(0≧x<∞) (6)
κ=ρc/k, (7)
u(x,t=0)=u0, (8)
∂u/∂x−hu=0 at x=0, (9)
Here, the solid is initially at temperature u=0 and is heated by radiation by a source at temperature u0. One solution for this formulation is set forth by H.S. Carslaw and J.C. Jaeger in Conduction of Heat in Solids, Oxford Press, 1946, pp. 70-73:
u(x,t)/u0=efrc(x/2√κt)−exp(hx+h 2 κt)erfc{x/2√κt+h√κt}, (10)
erfc(w)=1−(2/√π)∫w ∞exp(−v 2)dv. (11)
Adjacent to the boundary, x≈0, the radiation energy deposit in a volume ΔV corresponds to Eq. (9), and the heat energy continues to rise at and near this boundary as long as heat transfer across this boundary continues.
s=x/√4κt(s=0, 0.1, 0.2, . . . , 1.5) (12)
0≦x≦x(thr;1)=x(thr;ΔE1), (13)
for which the corresponding heat energy satisfies
(ρc)u(x≦x(thr;1),t)≧ΔE1. (14)
Phase change, once begun, is completed for a portion of the solid defined by condition
0≦x≦x(thr;2)=x(thr;ΔE1+ΔE2)≦x(thr;1), (15)
for which the corresponding heat energy satisfies
(ρc)u(x≦x(thr;2),t)≧ΔE1+ΔE2. (16)
t(thr;2)=t(x;ΔE1+E2), (17)
(ρc)u(x,t≧t(thr;2))≧ΔE1+ΔE, (18)
where the threshold time value t(x;ΔE1+E2) corresponds to completion of phase change at that value of the coordinate x, and t(x; ΔE1+ΔE2) increases monotonically with increasing x.
s(surv)=τ/√4κΔt(surv) (19)
of the dimensionless variable s is computed and compared with the horizontal line ψ=ψ0 in
is a fraction f (0<f<1) of the total projected area A of the exposed surface.
which is bounded by
f·OR(bulk)≦OR(area A)≦f·OR(photonic), (22)
where f is the area fraction determined in Eq. (20). An estimate of incident radiation energy E(rad;HS) received at the heat shield HS, that is reflected by the collection of clusters of transformed diatom material is
E(refl;HS)={1−OR(area A)}·E(rad;HS). (23)
Conclusion.
A(hex)=(6 d12)/√3. (A-1)
Where a single pore of radius d2 is located within this hexagon, the porosity fraction associated with this pattern has a value
porosity=(π√3/6)(d 2 /d 1)2(d 2 <d 1). (A-2)
A hydrofluoric acid (HF) solution can be used to increase the pore diameters d(pore) for a given diatom. It is unclear what effect, if any, an HF treatment has on the pore-to-pore separation distance d(p-p).
d(pore=45±9 nm,
porosity=7.5±1.2%,
d(p-p)=310 nm (estimate).
Three porous layers of silica are present, and the pore distribution is approximately radially symmetric for Coscinodiscus sp. For the T. eccentrica diatom, the corresponding dimensions were
d(pore)=40±6 nm,
porosity=10±2.5%,
d(p-p)=240 nm (estimate).
Claims (12)
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| SE2130098A1 (en) * | 2021-04-09 | 2022-10-10 | Swedish Algae Factory Ab | Photovoltaic device and anti-reflective coating comprising diatom frustules |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
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| SE2130098A1 (en) * | 2021-04-09 | 2022-10-10 | Swedish Algae Factory Ab | Photovoltaic device and anti-reflective coating comprising diatom frustules |
| SE544820C2 (en) * | 2021-04-09 | 2022-12-06 | Swedish Algae Factory Ab | Photovoltaic device and anti-reflective coating comprising diatom frustules |
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